Graduate Jobs at Icon plc
“ICON seeks a Senior Statistical Programmer to lead statistical programming tasks using R and SAS, analyze clinical trial data, collaborate with biostatisticians, and ensure high-quality regulatory reporting. Requires a degree in statistics/computer science, proficiency in SAS/R, and strong analytical skills. Competitive salary and benefits included.”
“Regular job offer at ICON for a Study Start Up Associate II role in clinical research. Requires 2+ years of experience in site start-up, BS degree, and skills in document review, compliance, and team collaboration. Competitive benefits and inclusive workplace culture.”
“ICON is hiring a Site Contracts Negotiator II for Mexico City. The role involves negotiating clinical trial agreements and budgets, managing contracts, and collaborating with internal teams. Requires a bachelor's degree in law, business, or related field, and contract negotiation experience. Remote position with competitive salary and benefits.”
“Regular full-time Site Specialist I role in Warsaw, Poland, supporting clinical trial site management and operations. Requires a Bachelor's degree in life sciences/healthcare/business, strong organizational skills, and experience in clinical research or administration. Offers competitive salary, benefits, and career development at ICON, a global healthcare research organization.”
“ICON seeks a remote Site Selection Specialist in Brazil to identify and build relationships with clinical study investigators/sites. Requires a Bachelor's degree, clinical research experience, and advanced English. Role involves feasibility assessments, data collection, and cross-functional collaboration. Competitive salary, health benefits, and performance incentives offered.”
“ICON seeks a Biospecimen Operations Manager to coordinate clinical trial sample handling, logistics, and regulatory compliance. Requires 2+ years in clinical drug development, hybrid role in Wilmington DE, strong cross-functional collaboration, and knowledge of ICH/GCP standards.”
“ICON seeks a Clinical Trial Manager to oversee trial operations, ensuring compliance with regulations, managing budgets/timelines, and collaborating with stakeholders. Requires a science/medicine degree, trial management experience, and 25% travel. Competitive salary and benefits included.”
“ICON seeks a Project Manager for IRT systems with 4+ years in project management and clinical research. Role involves managing timelines, budgets, stakeholder communication, and system updates. Requires travel (10%) and legal work rights. Competitive salary, benefits, and career development offered.”
“ICON seeks a Clinical Trial Associate to coordinate and administer trials, ensuring regulatory compliance, managing documentation, and supporting cross-functional teams in advancing innovative treatments with a competitive salary and benefits package.”
Icon plc | Mexico City
| Health, English
“Senior Study Support Assistant role at ICON in Mexico City. Provides administrative and operational support for clinical studies, mentors junior staff, and requires clinical trial management experience. Hybrid position with 5% travel. Competitive benefits package offered.”
“Regular job offer for Site Management Associate I at ICON, a global healthcare research organization. Requires a Bachelor's degree in life sciences/healthcare, some clinical research experience preferred, and 25% travel. Competitive salary, benefits, and career development opportunities included.”
“Legal Counsel role at ICON, a global healthcare research organization, requiring a qualified solicitor with experience in pharmaceutical/biotech contracts. Responsibilities include drafting agreements, compliance support, and risk mitigation. Competitive benefits and inclusive workplace culture.”
Icon plc | Copenhagen
| Finance, English
“ICON seeks a Contract Analyst I to manage clinical trial agreements, budgets, and negotiations with sites. Requires 2+ years in clinical research contracting, strong negotiation, and organizational skills. Offers competitive salary, benefits, and career development in healthcare intelligence.”
“Regular job offer for a Site Contracts Negotiator II role in Budapest, Hungary. Requires fluent Hungarian and English, contract management experience, and negotiation skills. Offers competitive salary, benefits, and career development in a healthcare CRO.”
“ICON seeks a Study Support Assistant to provide administrative and operational support for clinical trials. Requires high school diploma (Bachelor's preferred), healthcare experience, and proficiency in Microsoft Office. Offers competitive salary, benefits, and career development in a values-driven global healthcare organization.”
“ICON seeks a Contract Analyst I to manage clinical trial site contracts, budgets, and negotiations. Requires 2+ years in clinical research contracting, ICH-GCP knowledge, and strong stakeholder skills. Offers competitive salary, benefits, and career growth in a global healthcare CRO.”
“ICON seeks a Contract Analyst I to manage clinical trial agreements, budgets, and negotiations with sites. Requires 2+ years in clinical research contracting, strong negotiation, and organizational skills. Offers competitive salary, benefits, and career development in a global healthcare research organization.”
“ICON seeks a Site Specialist II for home-based operations in Riga, Latvia. Role involves managing site support activities, ensuring clinical trial compliance, and coordinating documentation and logistics. Requires life sciences/healthcare degree or equivalent experience, GCP knowledge, and strong organizational skills. Competitive salary and benefits included.”
“ICON seeks a Contract Analyst I to manage clinical trial agreements, budgets, and negotiations with sites. Requires 2+ years in clinical research contracting, BS degree, and strong negotiation/organizational skills. Offers competitive salary, benefits, and career development in healthcare intelligence.”
“ICON seeks a Site Contracts Lead in Mexico for remote work. Role involves managing clinical trial agreements, budgets, and negotiations. Requires legal/business degree, contract management experience, and strong negotiation skills. Competitive benefits and inclusive workplace offered.”
“ICON seeks a Contract Analyst to manage site budgets, contracts, and negotiations for clinical trials. Requires 2+ years in clinical research contracting, strong negotiation and organizational skills. Offers competitive salary, benefits, and career development in a global healthcare research organization.”
“Regular full-time Informed Consent Specialist I role at ICON for Mexico and Colombia. Remote position requiring clinical research experience, regulatory knowledge, and document management skills. Offers competitive salary, benefits, and career development in healthcare intelligence.”
“Regular job offer for Site Specialist II at ICON, a global healthcare CRO. Requires life sciences/healthcare degree or equivalent experience, site support background, and knowledge of clinical trials/GCP. Competitive salary, benefits, and career development opportunities included.”
“ICON seeks a Contract Analyst I to manage clinical trial agreements, budgets, and negotiations with sites. Requires 2+ years in clinical research contracting, BS degree, and strong negotiation/organizational skills. Offers competitive salary, benefits, and career development in a global healthcare research organization.”
“ICON seeks a Clinical Trial Associate in Rome to coordinate/administer trials, ensure regulatory compliance, and support data analysis. Requires a scientific degree, clinical research experience, and on-site presence. Offers competitive salary, benefits, and career development.”
“Regular job offer at ICON as a Laboratory Project Coordinator I. Responsible for monitoring trials, generating reports, and managing lab records. Competitive salary, health benefits, and performance incentives. Equal opportunity employer with inclusive culture.”
“Regular job offer at ICON for a Study Start-up Associate II role. Requires 2+ years in clinical research site start-up, BS degree, and skills in Excel, Word, and PowerPoint. Involves leading clinical trial initiation, document review, and compliance with regulatory requirements.”
“ICON seeks a Site Contracts Negotiator II (remote or office-based) in Bulgaria/UK to independently negotiate clinical trial agreements and budgets with UK sites. Requires law/business/life sciences degree or equivalent experience, UK site contracting expertise, and strong negotiation/communication skills. Competitive salary, benefits, and career development offered.”
“ICON seeks an AI Portfolio Analyst in Dublin for hybrid work. Role involves managing AI initiatives, gathering business requirements, and supporting portfolio governance with reporting and coordination across teams. Requires business analysis experience and AI/ML knowledge.”
“Regular job offer for a Study Start Up Associate at ICON, a clinical research organization. Requires 2+ years in site start-up, BS degree, and expertise in clinical trial initiation, document review, and compliance. Offers competitive salary, benefits, and career development in healthcare intelligence.”
“ICON seeks a Contract Analyst I for home-based roles in Spain. Responsibilities include negotiating clinical trial agreements, budgets, and managing invoicing. Requires 2+ years in clinical research site contracting, BS degree, and strong negotiation/organizational skills. Benefits include competitive salary, health coverage, and learning opportunities.”
“Regular job offer for a Site Specialist I role at ICON, a global healthcare research organization. Requires a Bachelor's degree in life sciences or related field, clinical research experience, and strong organizational skills. Responsibilities include site management, document tracking, and collaboration with CRAs. Competitive benefits and inclusive workplace culture.”
“ICON seeks an IT Product Manager in Dublin for a hybrid role (60% office-based). Responsibilities include defining IT products/services, collaborating across teams, and ensuring user adoption. Requires strong product lifecycle knowledge, project methodologies, and communication skills. Competitive salary and benefits offered.”
“Regular job offer for a Laboratory Support Coordinator at ICON, a global healthcare research organization. Responsibilities include assisting in trial monitoring, generating reports, and creating study documents. Competitive salary, benefits, and inclusive work environment.”
Icon plc | Buenos Aires
| Health, English
“ICON seeks a Clinical Project Manager (FSP) to lead cross-functional teams, manage budgets/timelines, and deliver clinical research projects. Requires PMP/PRINCE2 certifications, leadership experience, and 30% travel. Competitive salary and benefits included.”
Icon plc | Netherlands
| Finance, English
“Regular Lab Analyst II position at ICON, a global healthcare research organization. Requires a Bachelor's degree in a relevant field and 2-4 years of laboratory experience. Responsibilities include conducting tests, maintaining equipment, and ensuring data integrity. Offers competitive benefits and career development opportunities.”
Icon plc | From home
| Management, English
“ICON seeks a remote Project Manager for Mexico to lead healthcare project delivery, coordinate teams, manage budgets, and ensure on-time, high-quality results. Requires strong project management experience, leadership, and stakeholder engagement. Competitive salary and benefits included.”
“Regular job offer for a Study Start Up Associate II role at ICON, a global healthcare research organization. Requires 2+ years in clinical research site start-up, BS degree, and proficiency in Microsoft Office. Responsibilities include site document review, approval, and activation to meet study timelines. Competitive salary and benefits package offered.”
“Regular job offer for a Study Start Up Associate II role at ICON, a global clinical research organization. Requires 2+ years in clinical research site start-up, regulatory compliance, and trial initiation. Remote position based in Spain with competitive salary, benefits, and career development opportunities.”
“ICON seeks a Clinical Data Coordinator II in Livingston, UK, for recent graduates and early-career professionals. Role involves supporting clinical trial design, managing eCRF/data reconciliation, and collaborating with cross-functional teams. Requires a relevant bachelor's degree, attention to detail, and knowledge of clinical data management systems and regulatory guidelines.”
“ICON seeks a Site Partner II to manage investigator site relationships, ensure timely regulatory submissions (CEP/CONEP), and coordinate site activations. Requires expertise in ethics submissions, ICF preparation, and ICH/GCP compliance. Hybrid role with competitive salary, benefits, and career development in clinical research.”
“Clinical Research Associate (CRA I) position at ICON, a global clinical research organization. Remote role based in Romania requiring university degree in medicine/science, ICH-GCP knowledge, and 60% travel. Responsibilities include study monitoring, documentation, and stakeholder coordination.”
Icon plc | Mexico City
| Health, English
“Laboratory Project Coordinator I role at ICON in Mexico City (hybrid). Supports clinical trial monitoring, report generation, and study document creation. Requires life sciences/healthcare degree, advanced English, and project management experience. Competitive salary, benefits, and career development included.”
“ICOM busca Clinical Site Associate en Bélgica para rol remoto. Apoyo en gestión de sitios clínicos, activación de estudios, documentación y coordinación con CRAs. Requiere experiencia en investigación clínica, dominio de inglés, neerlandés y francés, y habilidades organizativas. Paquete de beneficios competitivo.”
“Regular job offer for Study Start Up Associate II at ICON, a global clinical research organization. Requires 2+ years in clinical research site start-up, proficiency in essential documents, and strong organizational skills. Competitive salary, benefits, and career development opportunities in healthcare intelligence.”
“Site Contracts Lead role at ICON for overseeing clinical trial agreements and budgets. Remote or office-based position requiring contract management experience in healthcare/CRO. Key tasks include negotiation, team coordination, and compliance. Competitive benefits package offered.”
“Senior Site Contracts Negotiator (Spanish Speaker) en España, remoto, para ICON. Gestiona negociación y ejecución de acuerdos clínicos con sitios, revisa contratos y colabora con equipos legales/financieros. Requiere experiencia en contratación clínica, dominio de español/inglés y habilidades organizativas.”
“ICON seeks a Medical Technologist II specializing in Hematology to process, analyze, and report clinical trial patient samples in a high-quality laboratory environment. Requires a Bachelor's degree in Medical Laboratory Science, 2+ years of hematology experience, and strong attention to detail. Competitive salary, benefits, and career development opportunities in a global healthcare research organization.”
“Site Specialist II role supporting clinical research sites in the Nordic region (Sweden, Norway, Denmark, Finland). Requires fluency in English and at least one Nordic language. Involves site activation, documentation management, and coordination of trial logistics. Competitive benefits package offered.”
“Biosampling Project Manager role in Bulgaria for ICON, a global clinical research organization. Requires experience in biosample operations, biomarker programs, and clinical trial management. Offers competitive salary, benefits (healthcare, retirement, learning programs), and focuses on regulatory compliance and data integrity in drug development.”
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